Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_008807572.1 KVAR_RS22260 5-carboxymethyl-2-hydroxymuconate semialdehyde dehydrogenase
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000025465.1:WP_008807572.1 Length = 488 Score = 367 bits (943), Expect = e-106 Identities = 198/469 (42%), Positives = 284/469 (60%), Gaps = 19/469 (4%) Query: 54 FPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMDASHRGRLLNRLADLIE 113 F T NP+TGEV+ +VA G + ++++AV AA+ AF W + R RL+ RL DLI+ Sbjct: 19 FHTTNPATGEVLAEVASGGEAEINQAVAAAKEAFP---KWANLPMKERARLMRRLGDLID 75 Query: 114 RDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYHGKTIPIDGDFFSYTRH 173 ++ +AA+ET D G P + V + ++A + +GKT P+D +YT Sbjct: 76 QNVPEIAAMETADTGLPIHQTKNVLIPRASHNFEFFAEVCQQMNGKTYPVDDKMLNYTLV 135 Query: 174 EPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLTALYVANLIKEAGFPPG 233 +PVGVC + PWN P + WK+ P LA GN V+K++E +PLTA + L EAG P G Sbjct: 136 QPVGVCALVSPWNVPFMTATWKVAPCLALGNTAVLKMSELSPLTADRLGELALEAGIPAG 195 Query: 234 VVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGSSNLKRVTLELGGKSPNI 293 V+N+V G+G TAG A+ H DV V+FTG T GR I AG LK+ ++ELGGKSP + Sbjct: 196 VLNVVQGYGATAGDALVRHHDVRAVSFTGGTATGRNIMKNAG---LKKYSMELGGKSPVL 252 Query: 294 IMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFVQEDIYDEFVERSVARAKSRVVGNPFD 353 I DAD++ A++ A F +F G+ C AGSR F+Q+ IY EFV+R RA VG+P D Sbjct: 253 IFEDADIERALDAALFTIFSINGERCTAGSRIFIQQSIYPEFVKRFAERANRLRVGDPTD 312 Query: 354 SKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGGGIAADR----------GYFIQPTVF 403 T+ G + + ++K+ GYI G +EGA LL GG AD+ G F++PTV Sbjct: 313 PNTQVGALISKQHWEKVSGYIRLGIEEGATLLAGG---ADKPSDLPAHLKAGNFLRPTVL 369 Query: 404 GDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAAAVFTKDLDKANYLSQAL 463 DV + M +A+EEIFGPV +L FK E + AN+ YGLA+ ++T+D+ K L++ + Sbjct: 370 ADVDNRMRVAQEEIFGPVACLLPFKDEAEGLRLANDVEYGLASYIWTQDVSKVLRLARGI 429 Query: 464 QAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYTEVKTVTVKV 512 +AG V+VN +V + PFGG K SG+GRE GEY + + E+K V + + Sbjct: 430 EAGMVFVNTQNVRDLRQPFGGVKASGTGREGGEYSFEVFAEMKNVCISM 478 Lambda K H 0.319 0.136 0.409 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 603 Number of extensions: 22 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 517 Length of database: 488 Length adjustment: 34 Effective length of query: 483 Effective length of database: 454 Effective search space: 219282 Effective search space used: 219282 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory